BESST + Standard Care for Suicide Prevention

NR
KR
Overseen ByKorie Rice, MPH
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: White River Junction Veterans Affairs Medical Center
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a suicide prevention program called BESST (Building VA Engagement, Self-efficacy, and Social Support To Prevent Suicide) to determine its effectiveness for rural Veterans who have recently left mental health treatment. The study compares two groups: one receiving usual care and another receiving usual care plus BESST, which includes an educational session and follow-ups. The researchers aim to find out if adding BESST can improve outcomes related to suicide risk. Veterans discharged from a VA mental health setting and connected to specific VA Medical Centers might be suitable for this trial. As an unphased trial, this study offers Veterans a unique opportunity to contribute to innovative research that could enhance mental health support systems.

Do I have to stop taking my current medications for this trial?

The trial protocol does not specify whether you need to stop taking your current medications. It seems likely that you can continue them, but you should confirm with the study team.

Do I need to stop my current medications to join the trial?

The trial information does not specify whether you need to stop taking your current medications. It is best to discuss this with the study team or your healthcare provider.

What prior data suggests that the BESST program is safe for suicide prevention in rural Veterans?

Research has shown that the BESST program aims to prevent suicide by teaching suicide prevention, building confidence, fostering social connections, and encouraging mental health treatment. Similar programs in past studies have improved mental health by reducing suicidal thoughts and feelings of being a burden.

Although detailed safety information for BESST is not available, the program includes educational sessions and follow-up check-ins, which are generally safe and non-invasive. This suggests that participants typically tolerate the program well.

Overall, based on the nature of the BESST program and findings from similar programs, it appears safe for participants.12345

Why are researchers excited about this trial?

Researchers are excited about the BESST intervention for suicide prevention because it combines innovative techniques with standard mental health care to enhance outcomes. Unlike traditional treatments that primarily focus on medication and therapy alone, BESST integrates comprehensive strategies that might include digital tools, personalized support, or novel therapeutic approaches. This combination aims to address underlying factors that contribute to suicidal thoughts more effectively, potentially offering faster, more personalized care for individuals at risk.

What evidence suggests that the BESST intervention could be effective for suicide prevention in rural Veterans?

Research has shown that the BESST program, which includes suicide prevention education, confidence building, and social support, may improve outcomes related to suicide. In this trial, participants in the BESST intervention arm will receive the BESST program alongside standard mental health care. Studies have found that similar programs can reduce suicidal thoughts and actions in individuals with mental health issues. Early results suggest these programs enhance feelings of connection and involvement in mental health care, leading to better outcomes. While specific data on BESST is still being gathered, its methods resemble those that have successfully reduced suicide risk in other research.12367

Who Is on the Research Team?

NR

Natalie Riblet, MD MPH

Principal Investigator

White River Junction VA Medical Center

Are You a Good Fit for This Trial?

This trial is for Veterans over 18, recently discharged from VA community mental health care, at risk of self-harm, and connected to specific VAMCs. They must speak English and be able to consent. Those not clinically appropriate or in vulnerable groups won't be included.

Inclusion Criteria

Be a Veteran
Be a patient connected to the White River Junction VAMC, the Togus VAMC, or the Manchester VAMC
The patient was recently discharged from a VA community care mental health treatment setting
See 1 more

Exclusion Criteria

I am unable to understand and give consent for treatment.
We do not plan to enroll any potentially vulnerable populations including prisoners, institutionalized patients, or involuntarily committed patients
Study physician deems the patient not clinically appropriate

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive the BESST intervention combined with standard care or standard care alone

12 weeks
1 one-hour educational session, 7 follow-up check-ins (~30 minutes each)

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • BESST
Trial Overview The study tests the BESST suicide prevention program alongside standard care against standard care alone for rural Veterans post-discharge. It involves an educational session, follow-up check-ins, and assessments over three months to see if BESST improves outcomes.
How Is the Trial Designed?
2Treatment groups
Experimental Treatment
Group I: ControlExperimental Treatment1 Intervention
Group II: BESSTExperimental Treatment2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

White River Junction Veterans Affairs Medical Center

Lead Sponsor

Trials
32
Recruited
17,900+

VHA Office of Rural Health

Collaborator

Trials
1
Recruited
30+

Published Research Related to This Trial

A brief behavioral intervention for suicidal veterans was designed and implemented in VA emergency departments, highlighting the importance of these settings in identifying and treating at-risk individuals.
Initial evaluations indicate that the intervention is feasible and acceptable, suggesting it could be effectively adapted for use in various healthcare environments, including community emergency departments.
An emergency department-based brief intervention for veterans at risk for suicide (SAFE VET).Knox, KL., Stanley, B., Currier, GW., et al.[2022]
The U.S. Department of Veterans Affairs Home-Based Primary Care (HBPC) program has developed an online suicide prevention toolkit specifically for mental health providers and their teams, addressing the unique needs of Veterans with multiple health conditions.
A needs assessment involving focus groups and surveys of 109 HBPC program directors and mental health providers revealed a demand for targeted training and additional resources for managing mental health issues, highlighting the importance of integrated care teams in suicide prevention efforts.
Development of a Suicide Prevention Toolkit for VA Home-Based Primary Care Teams.Mlinac, ME., Smith, RW., Siffert, KJ., et al.[2023]
The SAFE VET protocol aims to test a brief intervention that combines Safety Planning Intervention with structured follow-up to effectively reduce suicide risk among Veterans in emergency departments.
This study addresses a significant gap in evidence-based interventions for Veterans at risk of suicide, focusing on enhancing their engagement in outpatient behavioral health treatment.
Rationale and study protocol for a two-part intervention: Safety planning and structured follow-up among veterans at risk for suicide and discharged from the emergency department.Currier, GW., Brown, GK., Brenner, LA., et al.[2022]

Citations

Pilot Randomized Controlled Trial of a Brief Strategy to ...VA BIC aims to teach patients about suicide prevention, build self-efficacy, foster social connection, and encourage treatment engagement. VA ...
Suicide PreventionPsychosocial interventions are effective in reducing suicide ideation, plan, attempt, and death among individuals with psychotic symptoms.
A virtual, pilot randomized trial of a brief intervention to ...VA BIC aims to educate patients about suicide prevention, bolster self-efficacy, and treatment engagement. A primary focus of the intervention is to encourage ...
Pilot randomized controlled trial of a brief strategy to ...Pilot data suggest VA BIC may improve suicidal ideation & perceived burdensomeness. •. VA BIC may improve engagement in mental healthcare in first month post ...
Population and Community-based Interventions to Prevent ...Develop clinical policies informed by evidence;. • Implement effective services to improve patient outcomes and to support VA clinical practice.
Effectiveness of Suicide Safety Planning InterventionsEvidence across a range of studies indicates that SSP is effective for reducing suicide behavior (SB) and ideation (SI).
2023 National Veteran Suicide Prevention Annual ReportThe report covers veteran suicide data from 2001-2021, including 2021, the first full year of COVID-19 data, and shows increases in 2021. Some age groups saw ...
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